Hydrophilized curable silicone impression materials with improved storage behavior

ABSTRACT

The invention relates to hydrophilized curable silicone compositions which contain organopolysiloxanes, hydrophilizers and at least one stabilizing phosphorous compound. The compositions are particularly suitable as curable impression materials in dental applications, especially as wash impression materials.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation of pending prior application Ser. No.11/993,535, filed Jun. 14, 2006, which is a national stage filing under35 U.S.C. 371 of PCT/US2006/023236, filed Jun. 14, 2006, which claimspriority to EP Application No. 05013474.1, filed Jun. 22, 2005, thedisclosures of which are incorporated by reference in their entiretyherein.

FIELD OF THE INVENTION

The invention relates to hydrophilized curable silicone compositionswhich contain, organopolysiloxanes, hydrophilizers and at least onestabilizing phosphorous compound. The compositions are particularlysuitable as curable impression materials in dental applications,especially as wash impression materials.

BACKGROUND OF THE INVENTION

Dental impression materials, e.g., VPS impression materials, are commonproducts which dentists use to make highly precise impressions ofpatients' teeth. One disadvantage of some impression materials is theirhydrophobic nature which may negatively impact the achievable accuracyof the detail of an impression under the moist conditions in a patientsmouth. To overcome this problem, surfactants have been added to VPSimpression materials to make those more hydrophilic. Many so called“hydrophilic” VPS impression materials are available in the market basedon this technology.

Hydrophilicity of an impression material can be determined by ameasurement of contact angles of drops of water on the surface of asample of the impression material either in the unset or in the setphase using a standard goniometer. Generally, the higher thehydrophilicity of a VPS impression material, the lower the contact angleis. As the addition of surfactant can affect hydrophilicity, the amountof surfactant can influence the degree of hydrophilicity and the contactangle of dental materials such as VPS impression materials.

Generally, it is believed that the hydrophilicity of an impressionmaterial should be as high as possible, so there has been a tendency todevelop VPS dental impression materials with increased amounts ofsurfactant to achieve as low contact angles as possible. However, simplyincreasing the amount of surfactant in a VPS impression material cancause other problems, for example, with respect to aging properties ofthe resulting dental materials.

Typically, VPS impression materials consist of two components—a basepaste and a catalyst paste—the latter including a highly reactiveplatinum catalyst. These pastes are often filled into and stored incartridges or foil bags. When a surfactant is present in the catalystpaste, interactions between the surfactant and the platinum catalyst maybe observed, which are believed to retard the curing reaction anddecrease the shelf life of the catalyst paste. Additionally, theproperties of the cured material may be negatively influenced by such aninteraction. Accordingly, it is usually necessary, to include only lowamounts of surfactant, if any at all, in the catalyst paste, and toinclude most or all of the surfactant in the base paste.

The base paste of a VPS impression materials can also contain vinylpolysiloxanes, polysiloxanes or oligosiloxanes with Si—H-groups andadditives like pigments, surfactants, plasticizers, retarders, etc.Without the presence of a platinum catalyst, the base paste should notcure because the platinum catalyst induces the hydrosilylation curingreaction of the curable components.

The retardation of curing in crosslinkable mixtures is described in U.S.Pat. No. 6,346,562 B1 and U.S. Pat. No. 6,300,455 B1. Both patentsdescribe certain addition-crosslinkable silicone rubber systems. Agenerally encountered problem with such systems is, according to U.S.Pat. No. 6,346,562 B1 and U.S. Pat. No. 6,300,455 B1, that once thereactive mixture has been prepared it will cure, even at roomtemperature. This is particularly problematic when the productionmachines to make the base and catalyst pastes are not running for arelatively long time as a result of technical malfunctions or othercauses. In such cases, the reactive silicone rubber mixture present inthe machines can crosslink at room temperature, clogging the machinesand necessitating very costly cleaning work before the machines can berestarted. For this reason, U.S. Pat. No. 6,346,562 B1 suggests theaddition of at least one phosphorus compound to the reaction mixture inorder to suppress curing of the mixture at room temperature. Thedocument neither relates to hydrophilized dental materials, nor tomaterials designed to crosslink at room temperature.

SUMMARY OF THE INVENTION

Generally, hydrophilized dental materials should have shelf life as longas possible in order to be able to store the dental material in higherquantities, without the material losing its characteristical featureswith regard to material properties before and after curing.

Thus, there is a need for curable dental compositions that can be highlyhydrophilized but at the same time possess good shelf life. There isalso a need for a curable composition that can be highly hydrophilized,possesses good shelf life and has a curing behaviour comparable to priorart, unstabilised materials with a lower hydrophilicity.

In one aspect, the invention relates to a material which is curable at atemperature below 50° C., comprising

-   -   (A) an organopolysiloxane composition comprising at least one        organopolysiloxane (A1) with at least two ethylenically        unsaturated groups per molecule as component A,    -   (B) at least one organohydrogenpolysiloxane with at least 3 SiH        groups per molecule as component B,    -   (C) optionally organopolysiloxanes without reactive substituents        as component C,    -   (D) at least one hydrophilizing agent as component D,    -   (E) at least one stabilizer containing at least one phosphorous        atom as component E,    -   (F) a catalyst for promoting the reaction between components A        and B as component F,    -   (G) optionally, dental additives, adjuvants and colorants as        component G, and    -   (H) optionally, silane compounds with at least 2 ethylenically        unsaturated groups as component H.

One advantage of the invention is that the compositions of the inventionhave both a relatively high hydrophilicity and show no, or a relativelylow level, of viscosity increase during extended storage of thecompositions. Thus, if provided in the form of a multi component dentalmaterial, like an impression material, with a base paste and a catalystpaste wherein at least one of of the pastes contains a relatively highamount of surfactant, the component with the high level of surfactantwill not prematurely cure during extended storage. In addition toimproved storage stability, some embodiments of the invention alsoexhibit good tear strength after curing. For example, some of thecurable compositions containing organopolysiloxane provide elastomerswith good tear strength upon curing and good storage stability as wellas sufficient hydrophilicity that they can be used as light body orultra light body wash materials for taking impressions, especiallytaking impressions within the oral cavity.

In a preferred embodiment the material according to the inventioncomprises:

-   -   about 5- about 70 wt.-% components A+B+H,    -   about 0- about 40 wt.-% component C,    -   about 0.5- about 10 wt.-% component D,    -   about 0.0001- about 0.1 wt.-% component E,    -   about 0.00005- about 0.05 wt.-% component F, calculated as        elemental platinum and related to the overall weight of the        material present with the compounds A to H,    -   about 0- about 70 wt.-% component G, and    -   about 0.1- about 50 wt.-% component H.

Surprisingly, it has been found that adding a stabilizer which containsa phosphorous atom to the curable material results in an improvedstorage behaviour of the material while the curing behaviour and thematerial properties remain basically unchanged.

The invention further relates to a method of making a dental impression,wherein a material according to the invention is used.

A component A, according to the invention, contains oneorganopolysiloxane or a mixture of two or more polysiloxanes. In thelatter case, the n polysiloxanes present in component A are named A1, A2. . . An, respectively.

A component B, according to the invention, contains oneorganohydrogenpolysiloxane with at least 3 SiH groups per molecule or amixture of two or more of such organohydrogenpolysiloxanes. In thelatter case, the n organohydrogenpolysiloxanes present in component Bcan be named B1, B2, . . . Bn, respectively.

A component C, according to the invention, can contain oneorganopolysiloxanes without reactive substituents or a mixture of two ormore of such organopolysiloxanes. In the latter case, the norganopolysiloxanes present in component C can be named C1, C2, . . .Cn, respectively.

A component D, according to the invention, contains one hydrophilizingagent without reactive substituents or a mixture of two or more of suchhydrophilizing agents. In the latter case, the n hydrophilizing agentspresent in component D can be named D1, D2, . . . Dn, respectively.

A component E, according to the invention, contains one stabilizercontaining at least one phosphorous atom or a mixture of two or more ofsuch stabilizers. In the latter case, the n stabilizers present incomponent E can be named E1, E2, . . .En, respectively.

A component F, according to the invention, contains a catalyst forpromoting the reaction between components A and B or a mixture of two ormore of such catalysts. In the latter case, the n catalysts present incomponent F can be named F1, F2, . . .Fn, respectively.

A component G, according to the invention, contains one or more dentaladditives, adjuvants or colorants or a mixture of two or more of suchcompounds. In the latter case, the n catalysts present in component Gcan be named G1, G2, . . .Gn, respectively.

A component H, according to the invention, contains one silane compoundwith at least 2 ethylenically unsaturated groups or a mixture of two ormore of such compounds. In the latter case, the n silane compounds withat least 2 ethylenically unsaturated groups present in component H canbe named H1, H2, . . .Hn, respectively.

The invention also relates to a method for the preparation of a materialaccording to the present invention, wherein components A, B, D, E, and Fand optionally one ore more of components C, E and G and H are mixed.

The invention also relates to a method for the preparation of a materialin a two component dosage, wherein component B and components A, D and Eand one or more of components G and H are mixed to form a base paste andcomponent F and one or more of components A, C and G and H are mixed toform a catalyst paste.

The preparation according to the invention can be performed manually orautomated, especially supported by an appropriate dispensing cartridge.The present invention thus further relates to a method for thepreparation of a material according to the invention using a multiplecomponent dispensing cartridge, wherein the cartridge comprises multiplecompartments and at least one compartment contains component B andcomponents A, D and E and one or more of components G and H as a basepaste and at least one other compartment contains component F and one ormore of components A, C and G and H as a catalyst paste and wherein thematerial in the compartments is mixed upon manual or automated actionupon the compartments to form a material according to the invention.

The invention further relates to a kit of parts comprising at least twocontainers, wherein one container comprises component B and componentsA, D and E and optionally one or more of components C, G and H as a basepaste and at least one other container comprises component F and one ormore of components A, C and G and H as a catalyst paste.

The invention further relates to the use of a curable dental impressionmaterial comprising:

-   -   (A) at least one organopolysiloxane A1 with at least two        ethylenically unsaturated groups per molecule as component A,    -   (B) at least one organohydrogenpolysiloxane with at least 3 SiH        groups per molecule as component B,    -   (C) optionally organopolysiloxanes without reactive substituents        as component C    -   (D) at least one hydrophilizing agent as component D,    -   (E) at least one stabilizer containing at least one phosphorous        atom as component E,    -   (F) a catalyst for promoting the reaction between A and B as        component F and    -   (G) optionally dental additives, adjuvants and colorants as        component G and    -   (H) optionally silane compounds with at least 2 ethylenically        unsaturated groups as a component H        for the preparation of impression materials in dental        applications. The curable material can, e.g., comprise a mixture        of component C and G or mixture of component G an H or a mixture        of components C, G and H.

The invention further relates to a method for obtaining dentalimpressions, wherein a curable dental impression material comprising:

-   -   (A) at least one organopolysiloxane A1 with at least two        ethylenically unsaturated groups per molecule as component A,    -   (B) at least one organohydrogenpolysiloxane with at least 3 SiH        groups per molecule as component B,    -   (C) optionally organopolysiloxanes without reactive substituents        as component C,    -   (D) at least one hydrophilizing agent as component D,    -   (E) at least one stabilizer containing at least one phosphorous        atom as component E,    -   (F) a catalyst for promoting the reaction between A and B as        component F and    -   (G) optionally dental additives, adjuvants and colorants as        component G and    -   (H) optionally silane compounds with at least 2 ethylenically        unsaturated groups as a component H        is contacted with a region in an oral cavity of a mammal such as        hard or soft dental tissue which is to be to be reproduced by an        impression. The curable material can, e.g., comprise a mixture        of component C and G or mixture of component G an H or a mixture        of components C, G and H.

MORE DETAILED DESCRIPTION OF THE INVENTION

Component A according to the invention comprises at least oneorganopolysiloxane A1 with at least two pendant or terminaltriorganosiloxy groups in which at least one of the three organic groupsis a group with an ethylenically unsaturated double bond. Generally, thegroups with an ethylenically unsaturated double bond can be located onany monomeric unit of the organopolysiloxane. It is, however, preferred,that the groups with an ethylenically unsaturated double bond arelocated on or at least near the terminal, monomeric units of the polymerchain of the organopolysiloxane. In another preferred embodiment, atleast two of the groups with an ethylenically unsaturated double bondare located on the terminal monomeric units of the polymer chain.

The term “monomeric units” as used throughout the present text relatesto repeating structural elements in the polymer that form the polymerbackbone, unless expressly stated otherwise.

Preferred organopolysiloxanes of this general structure are representedby the following formula

in which the radicals R, independently from each other, represent anon-substituted or substituted, monovalent hydrocarbon group with 1 to 6C atoms, which is preferably free from aliphatic multiple bonds andwhere n generally can be chosen such that the viscosity of theorganopolysiloxanes lies between about 4 and about 500,000 mPas orbetween about 6 and about 100,000 mPas. The parameter n can, e.g., be inthe range of about 10 to about 3000.

Generally, the radicals R in the above formula can represent anynon-substituted or substituted, monovalent hydrocarbon group with 1 to 6C atoms. Non-substituted or substituted, monovalent hydrocarbon groupswith 1 to 6 C atoms can be linear or, if the number of carbon atomsexceeds 2, branched or cyclic. Generally, the radicals R can be equippedwith any type of substituent or substituents provided they do notinterfere with any other constituents or substituents of the compositionand do not interfere with the curing reaction. The term “interfere” asused in the context of the present text relates to any influence of sucha substituent on at least one of the other substituents or constituentsof the composition or the curing reaction, or both, which is detrimentalto the properties of the hardened product. The term “detrimental” asused in the context of the present text relates to a change ofproperties of the precursors or the cured product that negatively affectthe usefulness of the precursors or the cured product in their intendeduse.

In another preferred embodiment of the invention, at least about 50% ofthe radicals R are methyl groups. Examples of other radicals R that canbe present in the organopolysiloxanes according to the above formula areethyl, propyl, isopropyl, n-butyl, tert.butyl, the pentyl isomers, thehexyl isomers, vinyl, propenyl, isopropenyl, 2- and 3-n-butenyl, thepentenyl isomers, the hexenyl isomers, fluorine substituted aliphaticradicals like 3,3,3-trifluoropropyl groups, cyclopentyl or cyclohexylgroups, cyclopentenyl or cyclohexenyl groups or aromatic orhereroaromatic groups like phenyl or substituted phenyl groups. Examplesfor such molecules are described in U.S. Pat. No. 4,035,453, thedisclosure of which, especially the disclosure of the latter documentregarding the above mentioned molecules, their chemical constitution andtheir preparation, is expressly regarded as being part of the disclosureof the present document and is included herein by reference.

The preparation of molecules according to the above-mentioned formulawould generally be understood by the skilled person based upon theteachings of the prior art regarding similar molecules.

Particularly preferred are linear polydimethylsiloxanes according to theabove formula, that have viscosities with the specified viscosity rangesand end groups comprising di-methylvinylsiloxy units and methyl groupsas the radicals R.

A component A which can be employed according to the invention canconsist of one type A1 of organopolysiloxane. The organopolysiloxane canhave a viscosity starting in the range of about 5 to about 500,000 mPas,or about 10 to about 50,000 mPas or about 30 to about 40,000 mPas, e.g.,a viscosity of about 50 to about 20,000 mPas, or from about 100 to about15,000 mPas or about 200 to about 10,000 mPas.

It is, however, also possible that component A comprises two or moreconstituents, A1, A2 and so on, which can differ, e.g., in the chemicalcomposition of their backbone, or their molecular weight, or theirsubstituents or their viscosity, or any other differentiating feature ortwo or more of the above mentioned features.

In one embodiment of the invention the difference in viscosities ofdifferent constituents of component A can be higher than a factor of 2,e.g., higher than a factor of about 5, higher than a factor of about 10,higher than a factor of about 20, higher than a factor of about 30,higher than a factor of about 40, higher than a factor of about 50,higher than a factor of about 60, higher than a factor of about 70,higher than a factor of about 80, higher than a factor of about 90 orhigher than a factor of about 100. The difference in viscosities can beeven higher, e.g., higher than a factor of about 200, higher than afactor of about 300, higher than a factor of about 500, higher than afactor of about 800, higher than a factor of about 1,000 or higher thana factor of about 5,000, it should, however, preferably not exceed avalue higher than a factor of about 10,000. It should be kept in mindthat the values mentioned above relate to a factor for the difference inviscosities, not the viscosity values themselves.

The constituent of A with the lowest viscosity of all constituents of Acan have a viscosity in the range of about 10 to about 1000 mPas, orabout 50 to about 500 mPas or about 100 to about 300 mPas. Theconstituent of A with the highest viscosity of all constituents of A canhave a viscosity of about 500 to about 500,000 mPas, e.g. from about1,000 to about 50,000 mPas or about 3,000 to about 20,000 mPas. Goodresults can e.g. be achieved when the constituent of A with the highestviscosity of all constituents of A has a viscosity of about 4,000 toabout 15,000 mPas, e.g. from about 5,000 to about 13,000 mPas or about6,000 to about 12,000 mPas.

In another embodiment of the invention, the component A can comprisethree constituents A1, A2 and A3. In this case, if the constituentsdiffer, e.g., in viscosity, the above mentioned definition for therelation of the viscosities of the constituent with the highestviscosity and the constituent with the lowest viscosity, A3 and A1, isalso applicable. The remaining constituent A2 can generally have anyviscosity with a value between the values for viscosity of A1 and A3.

A preferred method of measurement of the viscosity is performed withHaake Rotovisco RV20 (spindle MV, measuring cup NV). The viscosity ismeasured at 23° C. After activation and rectification of the system,spindle MV is installed. Then the material to be measured is filled intothe measuring cup NV. Without undue delay, the spindle is lowered intothe measuring cup NV. The spindle should be covered by a layer of thematerial of a maximum thickness of 1 mm. The material to be measured istempered for 20 min at 23° C. The measurement is started by starting thespindle to turn and the viscosity values (mPas) are recorded starting 20s after the start of measurement. Care must be exercised to ensure thatthe measuring cup NV does not rotate or move at any time. A value forthe viscosity is obtained in mPas. The above mentioned method ofmeasurement corresponds to DIN 53018-1.

If component A contains constituents of different viscosities, the ratioof the amount of constituent with the lowest viscosity to the amount ofconstituent with the highest viscosity can be chosen relatively freely,depending on the desired properties of the precursors and the curedresin. It has, however, proven to be advantageous when the ratio of theamount of constituent with the lowest viscosity to the amount ofconstituent with the highest viscosity is within a range of from about1:20 to about 20:1, especially about 1:10 to about 10:1 or about 1:5 toabout 5:1. Good results can e.g. be obtained with ratios of from about1:3 to about 3:1 or about 1:2 to about 2:1. It has furthermore provenadequate in some cases, when the amount of constituent with the highestviscosity is about equal to or higher than the amount of constituentwith the lowest viscosity, resulting in a value of from about 0.9:1 toabout 3:1 for the ratio of the amount of constituent with the highestviscosity to the amount of constituent with the lowest viscosity. All ofthe ratios are based on the weight of the constituents.

Component B comprises preferably an organohydrogenpolysiloxane with atleast 3 Si-bonded hydrogen atoms per molecule. By definition, anorganohydrogenpolysiloxane according to the present text does not belongto the group of organopolysiloxanes as described in the context of theinvention.

An organohydrogenpolysiloxane according to the invention preferablycontains about 0.01 to about 1.7 wt.-% silicon-bonded hydrogens. Thesilicon valencies which are not saturated with hydrogen or oxygen atomsare saturated with monovalent hydrocarbon radicals R which are free fromethylenically unsaturated bonds.

The hydrocarbon radicals R, may be selected independently from eachother, represent a linear or branched or cyclic, non-substituted orsubstituted, aliphatic or aromatic monovalent hydrocarbon groups with 1to 12 C atoms without ethylenically unsaturated bonds. In a preferredembodiment of the invention, at least about 50%, preferably about 100%,of the hydrocarbon radicals R that are bonded to silicon atoms aremethyl radicals.

Organohydrogenpolysiloxanes which can be suitable as component B or as aconstituents of component B can have a viscosity of about 10 to about1000 mPas or from about 15 to about 550 mPas or from about 20 to about150 mPas.

Suitable compounds for use in component C are organopolysiloxaneswithout reactive substituents. These are preferably linear, branched orcyclic organopolysiloxanes where all silicon atoms are surrounded byoxygen atoms or monovalent hydrocarbon radicals with 1 to18 carbon atomswhich can be substituted or non-substituted. The hydrocarbon radicalscan be methyl, ethyl, C₂-C₁₀ aliphatics, trifluoropropyl groups as wellas aromatic C₆-C₁₂ radicals.

Polydimethylsiloxanes with trimethylsiloxy end groups are particularlypreferred as a constituent of component C. Component C is used in thematerial according to the invention preferably in an amount of about 0to about 40 wt.-%, preferably about 0 to about 20 wt.-% or about 0 toabout 10 wt.-%.

Hydrophilizing agents which can be employed as constituents of componentD, can generally be chosen freely from all types of surfactants whichimprove the hydrophilicity of a silicone material which is curable viahydrosilylation reaction while at the same time do not negatively impactthe material properties or curing behaviour of the material or at leastnot more than avoidable or tolerable. Useful surfactants which improvethe hydrophilicity of a silicone material according to the invention cangenerally be chosen from anionic, cationic or non-ionic surfactants ormixtures of two or more of such types of surfactants.

It is preferred that the material according to the invention comprises anonionic surfactant as a hydrophilizing agent or a mixture of two ormore non-ionic surfactants.

Component D comprises an agent or a plurality of agents which aregenerally capable of increasing the hydrophilic character to acomposition, for example as demonstrated by an increase in the wettingangle of a drop of water or an aqueous solution or dispersion (e.g. aplaster suspension or the like) on the material (in its cured or uncuredstate) over that wetting angle achieved on the same silicon compositionwithout component D.

The measurement of the wetting angle to determine the hydrophilicity ofimpression materials is described in DE 43 06 997 A, page 5, thecontents of this document with regard to this method of measurementbeing expressly mentioned by reference and being regarded as part of thedisclosure of the present text.

Preferably, the hydrophilizing agents of component D do not containreactive groups so that they are not incorporated into the polysiloxanenetwork.

Ethoxylized fatty alcohols which are e.g. described in EP 0 480 238 B1can be used as component D. Furthermore, the non-ionic perfluoralkylatedsurface-active substances described in WO 87/03001 can be used. Alsopreferred are the non-ionic surface-active substances which aredescribed in EP 0 268 347 B1, i.e. the nonylphenolethoxylates,polyethylene glycol-mono- and diesters, sorbitan esters as well aspolyethylene glycol- mono- and diethers listed therein. The contents ofthe latter documents with regard to hydrophilizing agents and theirpreparation is expressly mentioned by reference and is regarded as partof the disclosure of the invention.

In a further embodiment of the invention, the hydrophilizing agent or atleast one of the hydrophilizing agents, if component D comprises two ormore hydrophilizing agents, contains silicone moieties.

Suitable hydrophilizing agents can be wetting agents from the group ofhydrophilic silicone oils which are not capable of being covalentlyincorporated into the hardened polymer network. Suitable hydrophilizingagents are described in WO 87/03001 and in EP 0 231 420 B1, the contentsof which with regard to the hydrophilizing agents are expresslymentioned by reference and are regarded as part of the disclosure of theinvention.

Useful as hydrophilizing agents in component D are polyethercarbosilanes of the general formula Q-P—(OC_(n)H_(2n))_(x)-OT, in whichQ stands for R₃—Si— or

R₃—Si—(R″—SiR₂)_(a)—R′—SiR″_(2,)

where every R in the molecule can be the same or different and standsfor an aliphatic C₁-C₁₈, a cycloaliphatic C₆-C₁₂ or an aromatic C₆-C₁₂hydrocarbon radical, which can optionally be substituted by halogenatoms, R′ is a C₁-C₁₄ alkylene group, R″ is R in the case of a≠0 or is Ror R₃SiR′ in the case of a=0, and a=0-2; P stands for a C₂-C₁₈ alkylenegroup, preferably a C₂-C₁₄ alkylene group or A-R″′, where A represents aC₂-C₁₈ alkylene group and R′″ a functional group from the followinglist: —NHC(O)—, —NHC(O)—(CH2)_(n-1)—, —NHC(O)C(O)—,—NHC(O)(CH2)_(v)C(O)—, —OC(O)—, —OC(O)—(CH2)_(n-1)—, —OC(O)C(O)—,—OC(O)(CH₂)_(v)C(O)—, —OCH₂CH(OH)CH₂OC(O)(CH2)_(n-1)-,OCH₂CH(OH)CH₂OC(O)(CH2)_(v)C(O)— with v=1-12; T is H or stands for aC₁-C₄ alkyl radical or a C₁-C₄ acyl radical; x stands for a number from1 to 200 and n stands for an average number from 1 to 6, preferably 1 to4.

The polyether part can be a homopolymer, but can also be a statistical,alternating or block copolymer.

Hydrophilizers which can be advantageously used as a part of component Dor as component D, either alone or as a mixture of two or more thereof,can be found in U.S. Pat. No. 5,750,589 to Zech et al., col 2, I. 47 tocol. 3 I. 27 and col. 3, I. 49 to col. 4, I. 4 and col. 5, I. 7 to col.14, I. 20.

Other hydrophilizers which can be advantageously used as a part ofcomponent D or as component D, either alone or as a mixture of two ormore thereof, can be found in U.S. Pat. No. 4,657,959 to Bryan et al.,col. 4, I. 46 to col. 6. I. 52 as well as in EP 0 231 420 B1 to Gribi etal. p4, I. 1 to p. 5, I. 16 and in the examples.

U.S. Pat. No. 5,750,589, U.S. Pat. No. 4,657,959 and EP 0 231 420 B1 areexpressly described and cited herein as a source of disclosure forcompounds which can be used as component D according to the invention.The documents and especially their disclosure with regard tohydrophilizers at the citations given above are incorporated byreference and are considered as being a part of the disclosure of thepresent text.

Further preferred surfactants are exthoxylated surfactants containing asiloxane solubilizing group as described in U.S. Pat. No. 4,657,959, thedisclosure of which is incorporated herein by reference.

Suitable surfactants can have the following Formula

where each R is independently a monovalent hydrocarbyl radical with 1 to22 C-atoms, R¹ is a divalent hydrocarbylene radical 1 to 26 C-atoms,each R² is independently hydrogen or a lower hydroxyalkyl radical, R³ ishydrogen or a monovalent hydrocarbyl radical with 1 to 22 C-atoms, n andb are independently greater than or equal to zero, and m and a areindependently greater than or equal to one, with the proviso that a hasa sufficient value and b is small enough so that a cured composition o£the invention has the desired water contact angle.

Preferably R and R³ are —CH₃, R¹ is —C₃H₆-, R² is hydrogen, n is aboutzero or about one, m is about one to about five, a is about five toabout 20 and b is about 0.

Several of such ethoxylated surfactants are available from Union CarbideCorp. as “SILWET” surface active copolymers. Preferred surface activecopolymers include SILWET 35, SILWET L-77, L-7600 and L-7602. SILWETL-77 is an especially preferred ethoxylated surfactant which is believedto correspond to the above formula where R and R³ are —CH₃, R¹ is—C₃H₆—, R² is hydrogen, n is about zero or about one, m is about one orabout two, a is about seven, and b is about 0. Also possible is the useof MASIL® SF19, as obtainable from Lubrizol performance products,Spartanburg, US.

Also possible is the use of polyether carbosilanes selected from thegroup consisting of:

-   Et₃Si—(CH₂)₃—O—(C₂H₄O)y-CH₃, Et=Ethyl-   Et₃Si—CH₂—CH₂—O—(C₂H₄O)y-CH₃, Et=Ethyl-   (Me3Si—CH₂)₃Si—(CH₂)₃—O—(C₂H₄O)y-CH₃, Me=Methyl-   Me₃Si—CH₂—SiMe₂—(CH₂)₃—O—(C₂H₄O)y-CH₃, Me=Methyl-   (Me3Si—CH₂)₂SiMe—(CH₂)₃—O—(C₂H₄O)y-CH₃, Me=Methyl-   Me₃Si—(CH₂)₃O—(C₂H₄O)y—CH₃, Me=Methyl-   Me₃Si—CH₂—CH₂—O—(C₂H₄O)y-CH₃, Me=Methyl-   Ph₃Si—(CH₂)₃—O—(C₂H₄O)y-CH₃, Ph=phenyl-   Ph₃Si—CH₂—CH₂—O—(C₂H₄O)y-CH₃, Ph=phenyl-   Cy₃Si—(CH₂)₃—O—(C₂H₄O)y-CH₃, Cy=cyclohexyl-   Cy₃Si—CH₂—CH₂—O—(C₂H₄O)y-CH₃, Cy=cyclohexyl-   (C₆H₁₃)₃Si—(CH₂)₃—O—(C₂H₄O)y-CH₃-   (C₆H₁₃)₃Si—CH₂—CH₂—O—(C₄H₄O)y-CH₃ in which y conforms to the    relation: 5≦y≦20.

Hydrophilizers are preferably present in the materials according to theinvention in an amount of more than about 0.1% by weight, relating tothe weight of the whole material. It can be preferred if the amount ofcomponent D is in a range of from about 0.1 to about 15% by weight orfrom about 0.3 to about 12% by weight or from about 0.5 to about 8% byweight or from about 0.8 to about 7% by weight or from about 1 to about6% by weight or from about 1.2 to about 5% by weight or from about 1.5to about 4% by weight.

The wetting angle of a drop of water on the surface of a cured materialaccording to the invention measured after 10 seconds, is preferably lessthan about 40°, particularly preferably <about 20°, in particular <about10°.

Wetting contact angles can be measured as follows: About 2.5 g of baseand 2.5 g of catalyst paste are mixed together until uniform (about 30s). 5 g of mixed paste is placed in a metal mould (40 mm×30 mm×2 mm)between two sheets of polyethylene and pressed flat using a glass plate.The specimen is allowed to stand undisturbed until set (about 15minutes). The polyethylene sheets are removed, being careful not totouch the surface of the specimen, and the specimen placed on the tableof a gynometer DSA 10 (Krüss), a well known device for measuring contactangles. 5 μl of water are placed onto the surface of the specimen and anautomatic contact angle measurement is started using standard softwareof the gynometer. Measuring time is at least 10 s up to 200 s.

Component E can generally comprise any type of stabilizer containing atleast one phosphorous atom, provided it does not significantlydetrimentally impact the properties of the cured composition or its curerate or any other important properties of the material according to theinvention. Component E can contain one substance containing at least onephosphorous atom or a mixture of two or more substances containing atleast one phosphorous atom. The stabilizer can be organic or inorganicor a mixture of organic and inorganic stabilizers can be used ascomponent E. The stabilizer can also contain two or more phosphorousatoms.

It is particularly preferred that Component E comprises an organicstabilizer containing at least one phosphorous atom, and moreparticularly, an organic stabilizer selected from the group consistingof organo phosphines, organo-phosphites, organo-phosphonites,di(organo-phosphites), di(organo-phosphonites) and combinations thereof.

Also useful as compound E can be organophosphorous compounds of theformula R¹ _(n)P(OR)_(3-n) in which n=0, 1, 2 or 3, R=C₁-C₁₈-alkyl,C₆-C₃₀-aryl or C₇-C₃₁-alkylaryl and R¹=R or (CR′₂)_(m) or (C₆R′₄)_(m)with H═R or OR and m=10.

Especially useful can be, e.g., compounds according to the generalformula P(R)₃, wherein R can be the same or different andR=C₁-C₁₈-alkyl, C₆-C₃₀-aryl, C₇-C₃₁-alkylaryl, or OR¹ withR¹=C₁-C₁₈-alkyl, C₆-C₃₀-aryl, C₇-C₃₁-alkylaryl. The radicals R or R¹ canbe the same or different.

Moreover, representative stabilizers can have the following generalformula

in which R¹, R², R³, R⁴ and R⁵ can be the same or different and can beH, saturated or unsaturated, linear or branched C1-C18-alkyl,C6-C30-aryl or C7-C31-alkylaryl and R¹, R², R³, R⁴ and R⁵ can optionallybe substituted by groups such as amino, mono- or dial-kylamino,carboxyl, fluorine, chlorine, bromine, cyano, benzyl, phenyl or toluyl.Compounds which can be used as component E in the context of theinvention are disclosed in U.S. Pat. No. 6,300,455 B1 to Haselhorst etal. The disclosure of this document with regard to phosphorouscontaining compounds and their preparation is incorporated herein byreference and its disclosure is regarded as being part of the disclosureof the present text.

If component E is chosen from the compounds according to the formula R¹_(n)P(OR)_(3-n), n can be 0, 1, 2 or 3, R and R¹ can independently fromeach other be

with R″ independently from each other being H, C₁-C₁₆-alkyl, C₆-C₃₀-arylor C₇-C₃₁-alkylaryl, halogen (Hal), SiR₃, OR and the like, especially asdescribed in U.S. Pat. No. 6,346,562, the disclosure of this documentwith regard to phosphorous containing compounds and their preparation isincorporated herein by reference and the disclosure is regarded as beingpart of the disclosure of the present text.

Also useful as constituents of component E are diisodecylphenylphosphite(commercially available as Lankromark® LE76 by Akzo Nobel),diphenyl-2-ethylhexylphosphite (commercially available as Lankromark®LE98 by Akzo Nobel), diphenylisodecyl-phosphite (commercially availableas Lankromark® LE131 by Akzo Nobel), trisnonyl-phenylphosphite(commercially available as Lankromark® LE109 by Akzo Nobel),tris(isodecyl)phosphate (commercially available as Lankromark® LE164 byAkzo Nobel) or tris(tridecyl)phosphate (commercially available asLankromark® LE406 by Akzo Nobel) or mixtures of two or more of thesecompounds.

Particularly preferred as a constituent of component E is a compoundaccording to the formula

with z=2, Triphenylphosphite or Diisodecylphenylphosphite (commerciallyavailable as Lankromark LE 76® by Akzo Nobel).

The amount of Component E to be used in the material according to theinvention can be within a broad range as long as the desired effect onthe storage stability is achieved and side effects with regard to thematerial properties of the cured material or other properties of thematerial according to the invention are minor. It can be advantageous,if component E is present in the material according to the invention inan amount of from about 0.0001 to about 0.1% by weight, in relation tothe weight of the material itself. It can, however, be preferred, ifcomponent E is present in the material according to the invention in anamount of from about 0.0005 to about 0.05% by weight, or from about0,001 to about 0.03% by weight, in relation to the weight of thematerial itself.

If the material according to the invention is a multi componentmaterial, especially a material consisting of a base paste and acatalyst paste, component E is present in the base paste. It has thenproven to be successful if component E is present in the base paste inan amount of from about 0.0001 to about 0.1% by weight, in relation tothe weight of the material itself. It can, however, be preferred, ifcomponent E is present in the base paste in an amount of from about0.0005 to about 0.05% by weight, or from about 0.001 to about 0.02% byweight, in relation to the weight of the material itself.

The ratio of component D to component E can be within a range of fromabout 10:1 to about 5000:1, especially about 30:1 to about 1000:1 orabout 50 to 1 to about 600:1.

Component F preferably comprises a platinum complex which can beprepared from hexachloroplatinum acid by reduction withtetramethyldivinyldisiloxane. Such compounds are known to the skilledperson. Any other platinum compounds which catalyze or accelerateaddition cross-linking of silanes with ethylenically unsaturated doublebonds are also suitable. Platinum-siloxane complexes as described, e.g.in U.S. Pat. No. 3,715,334, U.S. Pat. No. 3,775,352 and U.S. Pat. No.3,814,730 are suitable, for example. The disclosure of these patentswith regard to platinum complexes and their preparation is explicitlymentioned and expressly regarded as part of the disclosure of thepresent text.

The platinum catalyst is preferably used in quantities of about 0.00005to about 0.05 wt.-%, particularly about 0.0002 to about 0.04 wt.-%, eachcalculated as elemental platinum and related to the overall weight ofthe material present with the components A to G.

To control the reactivity of the addition reaction and to preventpremature curing, it may be advantageous to add an inhibitor whichprevents the addition reaction for a specific period of time or slowsthe addition reaction down. Such inhibitors are known and described,e.g. in U.S. Pat No. 3,933,880, the disclosure of which regarding suchinhibitors and their preparation is expressly regarded as being part ofthe disclosure of the invention. Examples of such inhibitors areacetylenic unsaturated alcohols such as 3-methyl-l-butyne-3-ol,1-ethynylcyclohexane-l-ol, 3,5-dimethyl-l-hexyne-3-ol and3-methyl-l-pentyne-3-ol. Examples of inhibitors based an vinyl siloxaneare 1,1,3,3-tetramethyl-1 ,3-divinyl siloxane, 1,3,5,7-tetravinyl-1,3,5, 7-tetramethylcyclotetrasiloxane and poly-, oligo-and disiloxanes containing vinyl groups. The inhibitor is regarded asbeing a part of component F.

Furthermore, the dental materials according to the invention canoptionally comprise a component G, containing additives such as fillers,plasticizers, pigments, anti-oxidizing agents, release agents and thelike.

For example, a chemical system may be employed to diminish the presenceor degree of hydrogen outgassing which may be typically generated as aresult of the vinyl polymerization. The composition thus may comprise afinely divided platinum metal that scavenges for and takes up suchhydrogen. The Pt metal may be deposited upon a substantially insolublesalt having a surface area of between about 0.1 and about 40m²/g.Suitable salts are Barium sulphate, barium carbonate and calciumcarbonate of suitable particle sizes. Other substrates includediatomaceous earth, activated alumina, activated carbon and others. Theinorganic salts are especially preferred to imply improved stability tothe resulting materials incorporating them. Dispersed upon the salts isabout 0.2 to about 2 parts per million of platinum metal, based upon theweight of the catalyst component. It has been found that employment ofthe platinum metal dispersed upon inorganic salt particles substantiallyeliminates or diminishes hydrogen outgassing during curing of dentalsilicones. Also Pd metal as described e.g. in DE 29 26 405 C3 or Pdcompounds as disclosed in to WO 97/37632 can be employed.

The compositions of the invention can also include a filler as componentG or part of component G, e.g., a mixture of fillers. A wide variety ofinorganic, hydrophilic or hydrophobic fillers may be employed such assilicas, aluminas, magnesias, titanias, inorganic salts, metallic oxidesand glasses. It has been found to be possible to employ mixtures ofsilicone dioxides, including those derived from crystalline siliconedioxide, such as pulverized quartz (4-6 μm); amorphous siliconedioxides, such as a diatomaceous earth (4-7 μm); and silanated fumedsilica, such as Cab-o-Sil TS-530 (160-240 m²/g), manufactured by CabotCorporation.

The sizes and surface areas of the foregoing materials are controlled tocontrol the viscosity and thixotropicity of the resulting compositions.Some or all of the foregoing hydrophobic fillers may be superficiallytreated with one or more silanating agents, as known to those ofordinary skill in the art. Such silanating may be accomplished throughuse of known halogenated silanes or alkoxysilanes or silazanes. Suchfillers can be present in amounts of from about 0 to about 65% byweight, especially about 5 to about 55 or about 20 to about 50 wt.-% ofthe material.

Among the fillers which can be used according to component G are fillerssuch as quarz, cristobalite, calcium silicate, diatomaceous earth,zirconium silicate, montmoril-lonite such as bentonite, zeolite,including molecular sieves such as sodium aluminium silicate, metaloxide powder such as aluminium or zinc oxide or their mixed oxides,barium sulphate, calcium carbonate, plaster, glass and plastic powder.

Suitable fillers are also pyrogenic or precipitated silicic acid andsilica aluminium mixed oxides. The above mentioned fillers can behydrophobized, for example by treatment with organosilanes or siloxanesor by the etherification of hydroxyl groups to alkoxy groups. One typeof filler or also a mixture of at least two fillers can be used. Theparticle distribution is preferably chosen such that there are nofillers with particle sizes of more than about 50 μm.

The overall content of fillers is in the range from about 0 to about90%, preferably about 30 to about 80%, with regard to components A to H.

A combination of reinforcing and non-reinforcing fillers is particularlypreferred. In this respect, the quantity of reinforcing fillers rangesfrom about 1 to about 10 wt.-%, in particular from about 2 to about 5wt.-%.

The difference in the named overall ranges, i.e. about 9 to about 70wt.-%, in particular about 28 to about 55 wt.-%, is accounted for bynon-reinforcing fillers.

Pyrogenically-prepared highly-disperse silicic acids which havepreferably been hydrophobized by surface treatment are preferred asreinforcing fillers. The surface treatment can be carried out, forexample with dimethyldichlorosilane, hexamethyldisilazane,tetramethylcyclotetrasiloxane or polymethylsiloxane.

Particularly preferred non-reinforcing fillers are quartzes,cristobalites and sodium aluminium silicates which can besurface-treated. The surface treatment can generally be carried out withthe same methods as described in the case of the strengthening fillers.

The material according to the invention can also optionally containsilane compounds with at least 2 ethylenically unsaturated groups as acomponent H. Preferred silane compounds follow the general formula

Si(R¹)_(n)(R²)_(4-n)

wherein R¹ is a linear, branched or cyclic monovalent ethylenicallyunsaturated substituent which can undergo an addition reaction withSiH-groups, having from 2 to 12 carbon atoms, R² is a monovalent radicalwithout groups that can undergo an addition reaction with SiH-groups orhave a detrimental influence on such a reaction with 1 to 12 carbonatoms and n is 2, 3 or 4. Especially preferred radicals R¹ are vinyl,allyl and propargyl, especially preferred radicals R² are linear orbranched C₁-C₁₂ alkyl groups. An example for a silane compound which canbe used according to the present invention is tetraallylsilane, whichcorresponds to the above formula when R¹ is equal to an allyl radicaland n is equal to 4.

Further preferred silane compounds follow the general formula:

(R¹)m(R²)_(3-m)Si—A-Si—(R¹)_(n)(R²)_(3-n)

wherein R¹ is a linear, branched or cyclic monovalent ethylenicallyunsaturated substituent which can undergo an addition reaction withSiH-groups, having from 2 to 12 carbon atoms, R² is a monovalent radicalwithout groups that can undergo an addition reaction with SiH-groups orhave a detrimental influence on such a reaction with 1 to 12 carbonatoms, a is a bivalent linear or branched or alicyclic, heterocyclic,aromatic or heteroaromatic group with 1 to about 10000 carbon atomswhich can contain nitrogen or oxygen atoms and m is 2 or 3, preferably3. Examples for bivalent radicals A are ethylene, propylene, butylene,penylene, hexylene, heptylene, octylene, nonylene, decylene,—H₂C—Ar—CH₂—, —C₂H₄—Ar—C₂H₄— with Ar being an aromatic bivalent radical,preferably phenyl, or bivalent polyether radicals of the general type—CH₂CH₂CH₂—O—[C₈H₂₈O]_(b)—CH₂CH₂CH₂— with 1≦a≦5 and 0≦b≦2000.

Also suitable as component H are silane dendrimers. Generally,three-dimensional, highly-ordered oligomer and polymer compounds aredescribed as dendrimers, which are synthesized starting from small coremolecules by a constantly repeating sequence of reactions. Monomer orpolymer molecules with at least one reactive site are suitable as a coremolecule. This is converted in a uni- or multi-level reaction with areactant which accumulates at the reactive site of the core molecule andfor its part has two new reactive sites. The conversion of core moleculeand reactant yields the core cell (generation zero). By repeating thereaction, the reactive sites in the first reactant layer are convertedwith further reactants, again at least two new branching sites beingintroduced into the molecule each time (1^(st) generation).

The progressive branching leads to a geometrical growth of the number ofatoms for each generation. As the overall size can only grow linearlybecause of the number of possible covalent bonds specified by thereactants, the molecules become more tightly packed from generation togeneration and they change their shape from starfish-shaped tospherical. Dendrimers of the zero and each further generation can bedendrimers used as component H according to the invention. Preferred arethose of the first generation although those of much higher generationscan be used.

Dendrimers of the first or higher generations are obtained as a coremolecule by conversion of tri- or tetraalkenyl silanes (preferably allyland vinyl) in a first step with hydro-genchloro-silanes. These productsare converted in a further step with alkenyl-Grignard compounds.

Particularly preferred in this case are dendrimers of the firstgeneration of the following formula:

SiR² _(x)((CH₂)_(n)—Si—((CH₂)_(m)—CH═CH₂)₃)_(4-x)

in which R² is defined as above, n=2, 3, 4 or 5, m=0, 1, 2 or 3, and x=0or 1.

Particularly preferred dendrimers according to this general formula are:

-   Me—Si((CH₂—CH₂—Si(vinyl)₃)₃-   Si((CH₂—CH_(z)-Si(vinyl)₃)₄-   Me—Si((CH₂—CH₂—CH₂—Si(allyl)₃)₃-   Si((CH₂—CH₂—CH₂—Si(allyl)₃)₄-   Me—Si((CH₂—CH₂—Si(allyl)₃)₃-   Si((CH₂—CH₂—Si(allyl)₃)₄-   Me—Si((CH₂—CH₂—CH₂—Si(vinyl)₃)₃-   Si((CH₂—CH₂—CH₂—Si(vinyl)₃)₄

A. W. van der Made and P. W. N. M. van Leeuwen describe the mainsynthesis of those silane dendrimers in J. Chem. Soc. Commen. (1992),page 1400 and in Adv. Mater. (1993), 5, no. 6, pages 366 ff. TheSynthesis begins for example with complete allylation oftetrachlorosilane to tetraallylsilane using 10% excess of allylmagnesium bromide in diethyl ether. In addition, the allyl groups arehydrosilylized with trichlorosilane in the presence of a platinumcatalyst.

Finally, the conversion takes place with allyl magnesium bromide indiethyl ether. As a result, a dendrimer is obtained with 12 allyl endgroups. This first generation can also be converted to a secondgeneration, 36 allyl groups being obtained. The Same topic is also dealtwith by D. Seyferth and D. Y Son in Organometallics (1994), 13,2682-2690.

Conversion products of tri- or tetra- or penta- or hexa- or hepta- oroctaal-kenyl(cyclo)siloxanes with hydrogenchloro-silanes are furthermorepossible as a core molecule. These are converted in a further step withalkenyl-Grignard compounds and lead to dendrimers with cyclical orlinear siloxane cores.

Both purified tri-, tetra-, penta-, hexa-, hepta- or octasiloxanedendrimers as well as any mixtures of those dendrimers can be usedaccording to the Invention.

Silane dendrimers, the preparation and use as varnishes of which areknown from DE 196 03 242 A1 and DE 195 17 838 A1 as well as from EP 0743 313 A1. Dendrimers listed there are also suitable for the purposeaccording to the invention. Polyfunctional alkenyl compounds arefurthermore suitable as cores.

Particularly suitable are trimethylolpropanetriallylether,tetrallylpentaerythrite, Santolink XI-100 (Monsanto),tetraallyloxyethane, 1,3,5-benzoltricarbonic acid triallyl ester,1,2,4-benzoltricarbonic acid triallylester, 1,2,4,5-benzoltetracarbonicacid tetrallylester, triallyl phosphate, triallyl citrate, triallylisocyanurate, triallyloxytriazine, hexaallylinosite, as well as generalcompounds which possess at least two ethylenically unsaturated groupswhich can be optionally substituted, for example O-allyl, N-allyl,O-vinyl, N-vinyl or p-vinylphenolether groups.

Possible polyenes are also described in U.S. Pat. No. 3,661,744 and EP 0188 880 A1. The polyene can have e.g. the following structure: (Y)—(X)m,m being an integer greater than or equal to 2, preferably 2, 3 or 4, andX being chosen from the —[RCR]_(f), —CR═CRR, —O—CR═CR—R, —S—CR═CR—R,—NR—CR═CR—R group, f being an integer from 1 to 9 and the R radicalshaving the meanings H, F, Cl, furyl, thienyl, pyridyl, phenyl andsubstituted phenyl, benzyl and substituted benzyl, alkyl and substitutedalkyl, alkoxy and substituted alkoxy as well as cycloalkyl andsubstituted cycloalkyl and each being able to be the same or different.(Y) is an at least difunctional organic radical which is constructedfrom atoms which are chosen from the C, O, N, Cl, Br, F, P, Si and Hgroup.

The allyl- and/or vinyl esters of the at least difunctional carbonicacids are for example very suitable polyene compounds. Suitable carbonicacids for this are those with carbon chains of 2 to 20 C atoms,preferably 5 to 15 C atoms. Allyl or vinyl esters of aromatic dicarbonicacids such as phthalic acid or trimellithic acid are also very suitable.Allyl ethers of polyfunctional alcohols, preferably at leasttrifunctional alcohols are also suitable. Allyl ethers of trimethylpropane, pentaerythrite triallyl ether or2,2-bis-oxyphenylpropane-bis-(diallyl phosphate) can be named asexamples. Compounds of the cyanuric acid triallylester, triallyltriazintrione type and similar are also suitable.

Dendrimers of the above mentioned type and their preparation aredescribed in U.S. Pat. No. 6,335,413 B1. The disclosure of this documentwith regard to such dendrimers and their preparation is expresslyregarded as part of the disclosure of the present invention.

According to the desired properties of the dental materials, thecomponent (H) is present in quantities of from about 0.01 to about 10wt.-%, preferably about 0.05 to about 5 wt.-% or about 0.1 to about 1wt.-%. Even the addition of very small amounts effects a considerableincrease in the tear strength of impression materials. In a preferredembodiment, component H ist present in the dental materials in an amountof about 0.1 to about 2 wt.-%, e.g. about 0.15 to less than about1wt.-%.

The quantity ratios of components A, B and H are preferably chosen suchthat about 0.5 to about 10 mol SiH units of component B are present permol of unsaturated double bond of components A and H. The amount ofcomponents A, H, and the B in the dental material is in the range offrom about 5 to about 70 wt.-% relative to the total weight of allcomponents. Preferably, the amount is in the range of from about 10 toabout 60 wt.-% and particularly in a range of from about 15 to about 55wt.-%.

The materials according to the invention are prepared by mixing thecomponents A to H and subsequently curing them in an addition reactiondesignated as hydrosilylizing in which, under the influence of theplatinum catalyst D, the SiH groups of the component B are added to theunsaturated groups of the components A and H respectively.

In a preferred embodiment the material according to the inventioncomprises:

-   -   about 5- about 70 wt.-% components A+B+H,    -   about 0- about 40 wt.-% component C,    -   about 0.5- about 10 wt.-% component D,    -   about 0.0001- about 0,1 wt.-% component E,    -   about 0.00005- about 0.05 wt.-% component F, calculated as        elemental platinum and related to the overall weight of the        material present with the compounds A to H,    -   about 0- about 70 wt.-% component G, and    -   about 0.1- about 50 wt.-% component H.

For reasons of storage stability, it can be preferable to formulate thematerials in a two-component dosage form in which the overall componentB is present in a so-called base paste. The overall component F ispresent physically separated from the base paste in a so-called catalystpaste. The components A or H or both can be either present in thecatalyst or base paste, respectively, preferably a part of each ofcomponents A and H respectively being present in the base paste and apart of components A or H in the catalyst paste. Components C and D arepresent in the base paste, however, minor amounts of component D canalso be present in the catalyst paste as long as the amount issufficiently small not to interfere with the curing ability of thecatalyst.

The invention thus also relates to a material, wherein said material ispresent in the form of a base paste and a catalyst paste physicallyseparated from it. The whole component B should be present in the basepaste and the whole component F should be present in the catalyst paste.Preferably at least a majority of component D and at least a majority ofcomponent E should be present in the base paste, preferably more thanabout 90% by weight or more, e.g., more than about 95, about 98, about99 or even about 100% by weight of components D and E should be presentin the base paste. The remaining components can be optionallydistributed in the two pastes.

The volume ratios of catalyst and base pastes can be about 10:1 to about1:10. A particularly preferred volume ratio of base paste:catalyst pasteis about 1:1. In the case of a volume ratio of about 1:1, the componentsA to H can be distributed as follows as base and catalyst paste.

TABLE 1 Total in base Base paste Catalyst paste and catalyst Component(wt.-%) (wt.-%) paste (wt.-%) (A) 10-60  10-60  10-60  (B) 2-60 — 1-30(C) 0-20 0-20 0-20 (D) 0.1-10  0-10 0.05-10   (E) 0.001-0.05  —0.0005-0.025  (F) — 0.00025-0.25   0.00005-0.05   (G) 0-70 0-70 0-70 (H)0-20 0-20 0-20

Preferred quantity ratios can be used as follows:

TABLE 2 Total in base Base paste Catalyst paste and catalyst Component(wt-%) (wt.-%) paste (wt.-%) (A) 20-55 20-55 20-55 (B)  5-20 — 2.5-10 (C)  0-10  0-10  0-10 (D) 0.5-5  0-5 0.25-5   (E) 0.005-0.03  —0.0025-0.015  (F) — 0.005-0.1  0.0025-0.05  (G) 20-60 30-65  25-62.5 (H)0-5 0-5 0-5

The base paste and catalyst paste can also be used in a ration of 5:1.With a volume ratio 5:1, both pastes can be filled into tubular filmbags and later, shortly before use, can be mixed using a mixing anddosing device such as PENTAMIX™ (3M ESPE). A dosage in the form ofdouble-chambered cartridges or capsules is also possible. Suitabledevices are, e.g., described in EP 0 232 733 A1, U.S. Pat. No.5,924,600, U.S. Pat. No. 6,135,631 and EP 0 863 088 A1, The citeddocuments are expressly mentioned as sources of disclosure for deliveryand handling devices such as film bags, mixing and dosing devices. Thecited documents are incorporated into the present text by reference andare the disclosure of the documents with regard to delivery and handlingdevices usable for curable materials according to the present inventionis regarded as being a part of the disclosure of the present text.

The compounds according to the present invention are generallyobtainable by mixing the respective components in the amounts givenabove. Generally, the mixing of the components can be performedmanually, e.g., by spatula or a manually operated multi compartmentdispenser, or automated, using one of the various available devicesavailable for such an automated task, preferably one of the devicesmentioned in EP 0 232 733 A1, U.S. Pat. No. 5,924,600, U.S. Pat. No.6,135,631 or EP 0 863 088 A1.

The materials according to the invention are particularly suitable asdental materials, especially as dental impression materials such asprecision impression materials, situation impression materials, biteimpression materials.

The materials of the invention preferably have tear strengths betweenabout 2.1 and about 8 MPa, and more preferably between about 2.4 andabout 5 MPa. It has, however, been found to be advantageous in somesituations, if the tear strength does not exceed a value greater thanabout 15 MPa. Generally, compositions with tear strength values betweenabout 2.1 and about 6 MPa, and especially between about 2.4 and about 5MPa, allow easy removability of the cured and imprinted material fromthe mouth without compromising details of the impression preparation.

The Materials according to the invention preferably have shore hardnessA values greater than or equal to about 40, preferably greater than orequal to about 45, and particularly preferably greater than or equal to≧about 50 with low processing viscosity and non-dripping consistencyaccording to ISO 4823. The upper limit for the shore A hardness of thecured materials according to the invention can be at a value of about70, or about 65.

The materials according to the invention exhibit an improved elasticity,measurable by an elongation of at least about 50%, preferably of atleast about 70%. Preferably the elongation of the materials according tothe invention is larger than about 100%, preferably larger than about200%

It is also a preferred feature of the materials according to theinvention that their consistency according to ISO 4823 is either in therange as described for heavy body materials, which is from about 25 toabout 35 or is in the range as described for light body materials, whichis greater than about 36 mm, preferably greater than about 37 mm orgreater than about 38 mm or greater than about 40 mm. Most preferredmaterials according to the invention exhibit a consistency of more thanabout 41 mm, e.g., between about 42 and about 48 mm. The upper limit forthe consistency according to ISO 4823 can be about 55 mm.

The invention is explained in further detail by the following examples.

EXAMPLES 1. Materials 1.1 Example A (Base Paste According to theInvention)

Compound Amount [%-weight] Vinyl-terminated Polydimethylsiloxanes, 4000cSt 46.000 Polymethylhydrogensiloxanes 12.000 Polydimethylsiloxane 5.995Hydrophobized fumed silica (100 m²/g) 4.000 Hydrophobized SiO₂ filler30.500 Triphenylphosphite 0.005 Carbosilane Surfactant 1.500

1.2 Example B (Catalyst Pate)

Compound Amount [%-weight] Vinyl-terminated Polydimethylsiloxane, 2000cSt 39.200 Polydimethylsiloxane 5.500 SiO₂ filler 50.000 Hydrophobizedfumed silica (100 m²/g) 3.100 Tetraallylsilane 0.500 PalladiumchlorideDispersion in silicone oil 0.100 Platinum catalyst solution 1.600

1.3 Example C (Comparative Base Paste Not According to the Invention)

Compound Amount [%-weight] Vinyl-terminated Polydimethylsiloxane, 4000cSt 46.000 Polymethylhydrogensiloxane 12.000 Polydimethylsiloxane 6.000Hydrophobized fumed silica (100 m²/g) 4.000 Hydrophobized SiO₂ filler30.500 Carbosilane Surfactant 1.500

2. Measurements

Tear strength:

Tear strength data were evaluated by tearing six I-shaped specimens witha central unit of 20 mm×4 mm×2 mm in a Zwick 1435 Universal testingmachine according to DIN 53504. The diameter of the samples was 6 mm andtheir length 50 mm. Base and catalyst pastes were mixed through a staticmixer and filled into a brass mold. After 24 hours at 23° C. thespecimen were removed, six measurements were made and the mean valuedetermined (speed 200 mm/min).

Setting times:

Setting time data are given for room temperature and evaluated using aShawburry Curometer. The end of the setting time was defined as the timeafter with the curing curve fell below the 10 mm line.

Shore hardness according to DIN 53505.

3. Properties

The following examples show that the effect of the stabilizerTriphenylphosphite in Example A on the curing reaction of the mixture ofbase and catalyst paste and on the properties of the set rubber comparedto the comparative example (Base Paste Example C).

Combination Tear Shore Hard- Setting time Base Catalyst Strength ness A10 at 23.0° C. Consistency pate pate (24 h) [MPa] min/24 h [min] [mm]Example A Example B 2.75 52/58 5.17 45 Example C Example B 2.67 53/585.92 45

4. Aging Studies 4.1 Viscosities of Examples

In the following examples base and catalyst pastes were filled intotypical two-chambered cartridges. Those were stored at elevatedtemperatures. After certain periods of storage at 70° C. and 50° C. thecartridges were re-examined. The data show the viscosities of the basepaste side of the cartridges.

Storage at 70° C.

Inventive Combination Comparison Combination Base Catalyst Base CatalystPaste Paste Paste Paste Example A Example B Example C Example B Start 9Pas 9 Pas 1 Week 8 Pas polymerised 1 Month 8 Pas 3 Months polymerised

Storage at 50° C.

Inventive Combination Comparison Combination Base Catalyst Base CatalystPaste Paste Paste Paste Example A Example B Example C Example B Start  9Pas  9 Pas  1 Week  9 Pas 13 Pas  1 Month  9 Pas 48 Pas  3 Months  8 PasPolymerised  6 Months 11 Pas  9 Months 15 Pas 12 Months 12 Pas 18 Months14 Pas 24 Months 17 Pas

These results show the effect of the organophosphorous compound on theviscosity of the base paste. At 50° C. even after 2 years there was nopreliminary polymerization of the base paste whereas the comparativeexample showed a polymerization of the base paste in the cartridge afteronly 3 months.

4.2 Stabiliser Tests

A solution consisting of the following components was produced toperform stabilization tests:

Component Amount [%] Vinyl-terminated Polydimethylsiloxane, 200 cSt82.1% Polymethylhydrogensiloxane 16.4% Carbosilane Surfactant 1.47%

To this basic solution, stabilisers were added and the solution wasstirred for 30 min. Then the test was stored in open glass beakers for16 h at 80° C.

Results:

Stabiliser Result None Polymerised 100 ppm DivinyltetramethyldisiloxanePolymerised  50 ppm Ionol Polymerised 100 ppm Ionol Polymerised 250 ppmIonol Polymerised 0.8% Vitamin E Polymerised 100 ppm Lankromark LE 76 NoViscosity Change 100 ppm Triphenylphosphite No Viscosity Change

These model experiments show the effect of organophosphorous compoundson the stability of reactive systems including a surfactant compared toother curing retarders or antioxidants.

1. Kit of parts comprising at least two containers, wherein onecontainer is a base paste container that contains a base pastecomprising: (A) at least one organopolysiloxane A1 with at least twoethylenically unsaturated groups per molecule as component A, (B) atleast one organohydrogenpolysiloxane with at least 3 SiH groups permolecule as component B, (D) at least one hydrophilizing agent ascomponent D, (E) at least one stabilizer containing at least onephosphorous atom as component E, and at least one other container is acatalyst paste container that contains a catalyst paste comprising: (A)at least one organopolysiloxane A1 with at least two ethylenicallyunsaturated groups per molecule as component A, and (F) a catalyst forpromoting the reaction between A and B as component F.
 2. The kit ofclaim 1, wherein the hydrophilizing agent is a surfactant.
 3. The kit ofclaim 2, wherein the surfactant is a non-ionic surfactant.
 4. The kit ofclaim 1, wherein the hydrophilizing agent contains silicone moieties. 5.The kit of claim 1, wherein the stabilizer is a compound of the formulaR¹ _(n)P(OR)_(3-n), n is 1, 2 or 3, R and R¹ can independently from eachother be

with R″ independently from each other being H, C₁-C₁₈-alkyl, C₆-C₃₀-arylor C₇-C₃₁-alkylaryl, halogen (Hal), or SiR₃.
 6. The kit of claim 5,wherein the stabilizer is a triarylphosphite.
 7. The kit of claim 6,wherein the stabilizer is triphenylphosphite.
 8. The kit of claim 5,wherein the stabilizer is diisodecylphenylphosphite.
 9. The kit of claim1, wherein the stabilizer is a compound of the formula

with z=2.
 10. The kit according to claim 1, wherein the kit furthercomprises at least one of: (C) organopolysiloxanes without reactivesubstituents as component C or (G) dental additives, adjuvants and/orcolorants as component G or (H) silane compounds with at least 2ethylenically unsaturated groups as component H, wherein components C,G, and H, when present, are optionally distributed in the base paste andthe catalyst paste.
 11. The kit according to claim 1, wherein said kitfurther comprises component H, wherein component H comprises a silane ofthe following formula:Si(R¹)_(n)(R²)_(4-n) wherein R¹ is a linear, branched or cyclicmonovalent ethylenically unsaturated substituent which can undergo anaddition reaction with SiH-groups, having from 2 to 12 carbon atoms, R²is a monovalent radical without groups that can undergo an additionreaction with SiH-groups or have a detrimental influence on such areaction with 1 to 12 carbon atoms and n is 2, 3 or 4, or whereincomponent H comprises a silane compound of the general formula:(R¹)_(m)(R²)_(3-m Si—A-Si—(R) ¹)_(m)(R²)_(3-m) wherein R¹ and R² areindependently from each other defined as above, A is a bivalent linearor branched or alicyclic, heterocyclic, aromatic or heteroaromatic groupwith 1 to 10000 carbon atoms which can contain nitrogen or oxygen atomsand m is 2 or 3, preferably 3 or wherein component H comprises adendrimer of the following formulaSiR² _(x)((CH₂)_(n)—Si—(CH₂)_(m)—CH═CH₂)₃)_(4-x) in which R² is definedas above, n=2, 3, 4 or 5, m=0, 1, 2 or 3, and x=0 or
 1. 12. The kitaccording to claim 1, wherein the volume ratio of base paste to catalystpaste is 10:1 to 1:10.
 13. A method of preparing a dental impressionmaterial, the method comprising: providing a kit according to claim 1;and mixing the base paste of the kit according to claim 1 with thecatalyst paste of the kit according to claim 1 to obtain the dentalimpression material.
 14. The method of claim 13, wherein the dentalimpression material has a consistency value according to ISO 4823 in arange from about 25 mm to about 35 mm.
 15. The method of claim 13,wherein the dental impression material has a consistency value accordingto ISO 4823 of greater than about 36 mm.
 16. The method of claim 13,wherein the dental impression material has a Shore hardness A value in arange from about 40 to about
 70. 17. The method of claim 13, wherein thedental impression material has a setting time at 23.0° C. in a range ofabout 5 minutes to about 6 minutes.
 18. The method of claim 13, whereinthe dental impression material has a tear strength value in a range fromabout 2.1 MPa to about 6 MPa.
 19. The method of claim 13, wherein thedental impression material is curable at a temperature below 50° C. 20.The method of claim 13, wherein the base paste container and thecatalyst paste container are each a film bag or are each one of twochambers in a double chamber cartridge.